Zobrazeno 1 - 10
of 22
pro vyhledávání: '"James S. Poole"'
Autor:
Samantha Y. Corrigan, James S. Poole
Publikováno v:
Journal of Physical Organic Chemistry. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4e8f3c2c4c7e040aa6f6516d24a3e11
https://doi.org/10.1002/poc.4442
https://doi.org/10.1002/poc.4442
Autor:
Abygail R. Waggoner, Yahya Abdulrahman, Alexis J. Iverson, Ethan P. Gibson, Mark A. Buckles, James S. Poole
Publikováno v:
Journal of Physical Organic Chemistry. 34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b9d9cd20ddbb9df605f778e62bd1c2c
https://doi.org/10.1002/poc.4299
https://doi.org/10.1002/poc.4299
Autor:
Yahya Abdulrahman, Abygail R. Waggoner, James S. Poole, Mark A. Buckles, Alexis J. Iverson, Ethan P. Gibson
Publikováno v:
Journal of Physical Organic Chemistry. 34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8df190f3b5ef38507d3b009c0f08c363
https://doi.org/10.1002/poc.4278
https://doi.org/10.1002/poc.4278
Autor:
Hoi Ling Luk, Christopher M. Hadad, Erica M. Johnson, Shijing Xia, Abygail R. Waggoner, James S. Poole
Publikováno v:
The Journal of Physical Chemistry A. 122:8326-8335
The effect of ring substitution on the kinetics of reaction of arenes, heterocycles, and alkenes with hydroxyl radical is investigated in terms of reactivity and selectivity, using laser flash photolysis (LFP) in acetonitrile solution. The LFP data i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b75536b7bbc257a34d44c93138954cfc
https://doi.org/10.1021/acs.jpca.8b08463
https://doi.org/10.1021/acs.jpca.8b08463
Publikováno v:
The Journal of organic chemistry. 84(6)
The regioselectivity of hydroxyl radical addition to arenes was studied using a novel analytical method capable of trapping radicals formed after the first elementary step of reaction, without alteration of the product distributions by secondary oxid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9605fcc58143306284bbe00c41fac415
https://pubmed.ncbi.nlm.nih.gov/30779577
https://pubmed.ncbi.nlm.nih.gov/30779577
Autor:
Alec Q. Ribblett, James S. Poole
Publikováno v:
The Journal of Physical Chemistry A. 120:4267-4276
The species 4-nitrenopyridine 1-oxide is known to exhibit triplet nitrene dominated chemistry to yield azo-dimer products exclusively, even at room temperature. As such, this species, and its analogue 4-nitrenoquinoline 1-oxide, are useful models to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74ce5f83ea75b348a59f0c0a59b992d7
https://doi.org/10.1021/acs.jpca.6b03025
https://doi.org/10.1021/acs.jpca.6b03025
Publikováno v:
International Journal of Mass Spectrometry. 378:69-75
Ion–molecule reactions in a flowing afterglow are used to examine the electronic structure of 3- and 4-pyridinylnitrene-n-oxide radical anions. Reactions with nitric oxide are generally similar to those reported previously for other aromatic nitren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bc12a9a87bb3e57113b5190e8f55e8a
https://doi.org/10.1016/j.ijms.2014.07.017
https://doi.org/10.1016/j.ijms.2014.07.017
Autor:
James S. Poole
Publikováno v:
Topics in Heterocyclic Chemistry ISBN: 9783319606866
The photochemistry of the heteroarene N-oxides and their derivatives is complex and multifaceted. This review discusses the photochemistry of heteroarene N-oxides in light of new studies of these species, as well as recent studies of nitrene intermed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01d6577b5b3d7946c6a472cab8d14891
https://doi.org/10.1007/7081_2017_4
https://doi.org/10.1007/7081_2017_4
Autor:
Larry Sallans, James S. Poole
Publikováno v:
Journal of Molecular Structure. 1003:41-46
The primary product of the photolysis of 4-azidoquinoline 1-oxide ( 1 ) is believed to be the azo-dimer ( 4 ), consistent with the photochemistry of the pyridine analogue ( 2 ). This species has not been unambiguously identified, and previous workers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98edaf2be0cc1e7e2d45b0f1cdfce3cc
https://doi.org/10.1016/j.molstruc.2011.07.006
https://doi.org/10.1016/j.molstruc.2011.07.006
Autor:
James S. Poole
Publikováno v:
Journal of Molecular Structure: THEOCHEM. 894:93-102
The photolysis of 3-azidopyridine 1-oxide in argon matrices leads to an unusual product distribution that consists of the triplet nitrene, 1,4-diazacyclohepta-2,3,5,7-tetraene 1-oxide (obtained from ring expansion) and 2,7-diazabicyclo[4.1.0]hepta-2,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd4e8546f2d9bc412924aadad5a9b812
https://doi.org/10.1016/j.theochem.2008.10.002
https://doi.org/10.1016/j.theochem.2008.10.002